NI200900031A - N-METHYLAMINOMETHYL ISOINDOL COMPOSITIONS AND COMPOSITIONS THAT INCLUDE THEM AND METHODS FOR USING THEM. - Google Patents

N-METHYLAMINOMETHYL ISOINDOL COMPOSITIONS AND COMPOSITIONS THAT INCLUDE THEM AND METHODS FOR USING THEM.

Info

Publication number
NI200900031A
NI200900031A NI200900031A NI200900031A NI200900031A NI 200900031 A NI200900031 A NI 200900031A NI 200900031 A NI200900031 A NI 200900031A NI 200900031 A NI200900031 A NI 200900031A NI 200900031 A NI200900031 A NI 200900031A
Authority
NI
Nicaragua
Prior art keywords
compositions
methylaminomethyl
methods
isoindol
compounds
Prior art date
Application number
NI200900031A
Other languages
Spanish (es)
Inventor
W Muller George
S C Chen Roger
Original Assignee
Celgene Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Celgene Corp filed Critical Celgene Corp
Publication of NI200900031A publication Critical patent/NI200900031A/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/4035Isoindoles, e.g. phthalimide
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • A61P15/04Drugs for genital or sexual disorders; Contraceptives for inducing labour or abortion; Uterotonics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00Antiparasitic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings

Abstract

La invención se refiere a compuestos de N-metilaminometil-isoindolina, y sales farmacéuticamente aceptables, solvatos, estereoisómeros, y profármacos de los mismos. Se describen métodos de uso, y composiciones farmacéuticas de estos compuestos.The invention relates to N-methylaminomethyl-isoindoline compounds, and pharmaceutically acceptable salts, solvates, stereoisomers, and prodrugs thereof. Methods of use, and pharmaceutical compositions of these compounds are described.

NI200900031A 2006-09-15 2009-03-13 N-METHYLAMINOMETHYL ISOINDOL COMPOSITIONS AND COMPOSITIONS THAT INCLUDE THEM AND METHODS FOR USING THEM. NI200900031A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US84522706P 2006-09-15 2006-09-15

Publications (1)

Publication Number Publication Date
NI200900031A true NI200900031A (en) 2010-02-01

Family

ID=38983295

Family Applications (1)

Application Number Title Priority Date Filing Date
NI200900031A NI200900031A (en) 2006-09-15 2009-03-13 N-METHYLAMINOMETHYL ISOINDOL COMPOSITIONS AND COMPOSITIONS THAT INCLUDE THEM AND METHODS FOR USING THEM.

Country Status (30)

Country Link
US (2) US8648096B2 (en)
EP (1) EP2076260B1 (en)
JP (1) JP5567339B2 (en)
KR (1) KR20090050107A (en)
CN (2) CN103382197A (en)
AR (1) AR062875A1 (en)
AT (1) ATE502634T1 (en)
CA (1) CA2663376C (en)
CL (1) CL2007002670A1 (en)
CO (1) CO6180446A2 (en)
CR (1) CR10696A (en)
CY (1) CY1112558T1 (en)
DE (1) DE602007013436D1 (en)
DK (1) DK2076260T3 (en)
ES (1) ES2361584T3 (en)
HR (1) HRP20110261T1 (en)
IL (1) IL197566A0 (en)
MX (1) MX2009002666A (en)
NI (1) NI200900031A (en)
NZ (1) NZ575689A (en)
PE (1) PE20080832A1 (en)
PL (1) PL2076260T3 (en)
PT (1) PT2076260E (en)
RS (1) RS51725B (en)
RU (1) RU2009114159A (en)
SI (1) SI2076260T1 (en)
TW (1) TW200819435A (en)
UA (1) UA95975C2 (en)
WO (1) WO2008033567A1 (en)
ZA (1) ZA200901852B (en)

Families Citing this family (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BRPI0514865A (en) * 2004-09-03 2008-06-24 Celgene Corp process for preparing a compound
ES2402204T3 (en) 2005-06-30 2013-04-29 Celgene Corporation Procedures for the preparation of 4-amino-2- (2,6-dioxopiperidin-3-yl) isoindoline-1,3-dione compounds
CN103382197A (en) * 2006-09-15 2013-11-06 细胞基因公司 N-methylaminomethyl isoindole compounds and compositions comprising and methods of using the same
US20100160368A1 (en) 2008-08-18 2010-06-24 Gregory Jefferson J Methods of Treating Dermatological Disorders and Inducing Interferon Biosynthesis With Shorter Durations of Imiquimod Therapy
SG195613A1 (en) * 2008-10-29 2013-12-30 Celgene Corp Isoindoline compounds for use in the treatment of cancer
US20110021555A1 (en) * 2008-12-19 2011-01-27 Graceway Pharmaceuticals, Llc Lower dosage strength imiquimod formulations and shorter dosing regimens for treating actinic keratoses
AU2010274097B2 (en) * 2009-07-13 2016-06-16 Medicis Pharmaceutical Corporation Lower dosage strength imiquimod formulations and short dosing regimens for treating genital and perianal warts
EP3202460B1 (en) 2010-02-11 2019-06-12 Celgene Corporation Arylmethoxy isoindoline derivatives and compositions comprising and methods of using the same
WO2012135299A1 (en) 2011-03-28 2012-10-04 Deuteria Pharmaceuticals Inc 2',6'-dioxo-3'-deutero-piperdin-3-yl-isoindoline compounds
JP6359563B2 (en) 2013-01-14 2018-07-18 デュートルクス・リミテッド・ライアビリティ・カンパニーDeuteRx, LLC 3- (5-substituted-4-oxoquinazolin-3 (4H) -yl) -3-deuteropiperidine-2,6-dione derivatives
BR112015022785A2 (en) 2013-03-14 2017-07-18 Epizyme Inc compound; pharmaceutical composition; packaged pharmaceutical kit or article; method of inhibiting an arginine methyl transferase (rmt); method of modulating gene expression; transcription modulation method; and method of treating an rmt-mediated disorder
WO2014153172A1 (en) 2013-03-14 2014-09-25 Epizyme, Inc. Pyrazole derivatives as prmt1 inhibitors and uses thereof
EP2970134B1 (en) 2013-03-14 2018-02-28 Epizyme, Inc. Pyrazole derivatives as prmt1 inhibitors and uses thereof
US9765035B2 (en) 2013-03-14 2017-09-19 Epizyme, Inc. Arginine methyltransferase inhibitors and uses thereof
WO2014152833A1 (en) 2013-03-14 2014-09-25 Deuterx, Llc 3-(substituted-4-oxo-quinazolin-3(4h)-yl)-3-deutero-piperidine-2,6-dione derivatives
WO2014153214A1 (en) 2013-03-14 2014-09-25 Epizyme, Inc. Arginine methyl transferase inhibtors and uses thereof
US9023883B2 (en) 2013-03-14 2015-05-05 Epizyme, Inc. PRMT1 inhibitors and uses thereof
US20160031839A1 (en) 2013-03-14 2016-02-04 Epizyme, Inc. Arginine methyltransferase inhibitors and uses thereof
US9346761B2 (en) 2013-03-14 2016-05-24 Epizyme, Inc. Arginine methyltransferase inhibitors and uses thereof
EP2970181B1 (en) 2013-03-14 2017-06-07 Epizyme, Inc. Arginine methyltransferase inhibitors and uses thereof
US9120757B2 (en) 2013-03-14 2015-09-01 Epizyme, Inc. Arginine methyltransferase inhibitors and uses thereof
BR112015026006B1 (en) 2013-04-17 2022-10-18 Signal Pharmaceuticals, Llc USE OF A COMPOUND IN COMBINATION WITH AN IMID® IMMUNOMODULATING DRUG FOR THE TREATMENT OR PREVENTION OF CANCER, PHARMACEUTICAL COMPOSITION AND KIT COMPRISING SUCH COMPOUNDS
UA117141C2 (en) 2013-10-08 2018-06-25 Селджин Корпорейшн Formulations of (s)-3-(4-((4-(morpholinomethyl)benzyloxy)-1-oxoisoindolin-2-yl)piperidine-2,6-dione
EA037738B1 (en) 2014-08-07 2021-05-17 Калитера Байосайенсиз, Инк. Crystal forms of glutaminase inhibitors
DK3643709T3 (en) * 2014-10-30 2021-12-20 Kangpu Biopharmaceuticals Inc ISOINDOLINE DERIVATIVE, INTERMEDIATE PRODUCT, METHOD OF MANUFACTURE, PHARMACEUTICAL COMPOSITION AND USE
US9809603B1 (en) 2015-08-18 2017-11-07 Deuterx, Llc Deuterium-enriched isoindolinonyl-piperidinonyl conjugates and oxoquinazolin-3(4H)-yl-piperidinonyl conjugates and methods of treating medical disorders using same
WO2017040376A1 (en) * 2015-08-31 2017-03-09 The University Of Toledo Potent phthalate inhibitors of aspartate n-acetyltransferase and selective aspartate pathway inhibitors
US10011566B2 (en) 2015-12-15 2018-07-03 Astrazeneca Ab Compounds
EP3440082A1 (en) * 2016-04-06 2019-02-13 The Regents of The University of Michigan Monofunctional intermediates for ligand-dependent target protein degradation
EP3454862A4 (en) 2016-05-10 2020-02-12 C4 Therapeutics, Inc. Spirocyclic degronimers for target protein degradation
WO2017197055A1 (en) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. Heterocyclic degronimers for target protein degradation
CN109641874A (en) 2016-05-10 2019-04-16 C4医药公司 C for target protein degradation3The glutarimide degron body of carbon connection
SG11201903483VA (en) 2016-10-28 2019-05-30 Icahn School Med Mount Sinai Compositions and methods for treating ezh2-mediated cancer
US11541051B2 (en) 2016-12-08 2023-01-03 Icahn School Of Medicine At Mount Sinai Compositions and methods for treating CDK4/6-mediated cancer
EP3638661A1 (en) 2017-06-14 2020-04-22 Astrazeneca AB 2,3-dihydroisoindole-1-carboxamides useful as ror-gamma modulators
WO2018237026A1 (en) 2017-06-20 2018-12-27 C4 Therapeutics, Inc. N/o-linked degrons and degronimers for protein degradation
CN111278815B (en) 2017-09-04 2024-03-08 C4医药公司 Glutarimide
CN111315735B (en) 2017-09-04 2024-03-08 C4医药公司 Dihydrobenzimidazolone
EP3679028A1 (en) 2017-09-04 2020-07-15 C4 Therapeutics, Inc. Dihydroquinolinones
EP3710002A4 (en) 2017-11-16 2021-07-07 C4 Therapeutics, Inc. Degraders and degrons for targeted protein degradation
AU2019231689A1 (en) * 2018-03-06 2020-09-24 Icahn School Of Medicine At Mount Sinai Serine threonine kinase (AKT) degradation / disruption compounds and methods of use
EP3773576A4 (en) 2018-03-26 2021-12-29 C4 Therapeutics, Inc. Cereblon binders for the degradation of ikaros
WO2019204354A1 (en) 2018-04-16 2019-10-24 C4 Therapeutics, Inc. Spirocyclic compounds
HUE064340T2 (en) * 2018-04-23 2024-03-28 Celgene Corp Substituted 4-aminoisoindoline-1,3-dione compounds and their use for treating lymphoma
EP3578561A1 (en) 2018-06-04 2019-12-11 F. Hoffmann-La Roche AG Spiro compounds
WO2020210630A1 (en) 2019-04-12 2020-10-15 C4 Therapeutics, Inc. Tricyclic degraders of ikaros and aiolos
EP4048279A1 (en) 2019-10-21 2022-08-31 Celgene Corporation Methods of treating chronic lymphocytic leukemia using 2-(2,6-dioxopiperidin-3yl)-4-((2-fluoro-4-((3-morpholinoazetidin-1-yl)methyl)benzyl)amino)isoindoline-1. 3-dione
AU2020372333A1 (en) * 2019-10-21 2022-04-28 Celgene Corporation Methods for treating a hematological cancer and the use of companion biomarkers for 2-(2,6-Dioxopiperidin-3-yl)-4-((2-fluoro-4-((3-morpholinoazetidin-1-yl)methyl)benzyl)amino)isoindoline-1,3-dione
CN110746400B (en) * 2019-11-07 2021-12-17 郑州大学 Androgen receptor targeted fluorescent probe and preparation method thereof
JP2024504932A (en) 2021-01-13 2024-02-02 モンテ ローザ セラピューティクス, インコーポレイテッド isoindolinone compound
CN115504963A (en) * 2021-06-22 2022-12-23 苏州开拓药业股份有限公司 C-Myc protein degradation agent

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5635517B1 (en) * 1996-07-24 1999-06-29 Celgene Corp Method of reducing TNFalpha levels with amino substituted 2-(2,6-dioxopiperidin-3-YL)-1-oxo-and 1,3-dioxoisoindolines
US6281230B1 (en) * 1996-07-24 2001-08-28 Celgene Corporation Isoindolines, method of use, and pharmaceutical compositions
TR200101501T2 (en) * 1998-03-16 2002-06-21 Celgene Corporation 2- (2,6-dioxopiperidin-3-yl) isoindoline derivatives, their preparation and use as inhibitors of inflammatory cytokines.
US20030045552A1 (en) * 2000-12-27 2003-03-06 Robarge Michael J. Isoindole-imide compounds, compositions, and uses thereof
US7091353B2 (en) * 2000-12-27 2006-08-15 Celgene Corporation Isoindole-imide compounds, compositions, and uses thereof
US7323479B2 (en) * 2002-05-17 2008-01-29 Celgene Corporation Methods for treatment and management of brain cancer using 1-oxo-2-(2,6-dioxopiperidin-3-yl)-4-methylisoindoline
US7968569B2 (en) * 2002-05-17 2011-06-28 Celgene Corporation Methods for treatment of multiple myeloma using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione
EP1569907B1 (en) * 2002-12-13 2016-03-09 YM BioSciences Australia Pty Ltd Nicotinamide-based kinase inhibitors
US20050143344A1 (en) * 2003-12-30 2005-06-30 Zeldis Jerome B. Methods and compositions using immunomodulatory compounds for the treatment and management of central nervous system disorders or diseases
ES2402204T3 (en) * 2005-06-30 2013-04-29 Celgene Corporation Procedures for the preparation of 4-amino-2- (2,6-dioxopiperidin-3-yl) isoindoline-1,3-dione compounds
CN103382197A (en) * 2006-09-15 2013-11-06 细胞基因公司 N-methylaminomethyl isoindole compounds and compositions comprising and methods of using the same

Also Published As

Publication number Publication date
PT2076260E (en) 2011-06-07
AR062875A1 (en) 2008-12-10
ZA200901852B (en) 2010-06-30
CA2663376C (en) 2015-01-06
CY1112558T1 (en) 2016-02-10
KR20090050107A (en) 2009-05-19
PL2076260T3 (en) 2011-08-31
MX2009002666A (en) 2009-04-09
CN103382197A (en) 2013-11-06
NZ575689A (en) 2011-12-22
US8648096B2 (en) 2014-02-11
RU2009114159A (en) 2010-10-20
PE20080832A1 (en) 2008-08-06
CR10696A (en) 2009-05-13
CA2663376A1 (en) 2008-03-20
ES2361584T3 (en) 2011-06-20
JP2010503688A (en) 2010-02-04
US20080214615A1 (en) 2008-09-04
RS51725B (en) 2011-10-31
DE602007013436D1 (en) 2011-05-05
CL2007002670A1 (en) 2008-05-16
SI2076260T1 (en) 2011-05-31
TW200819435A (en) 2008-05-01
EP2076260B1 (en) 2011-03-23
HRP20110261T1 (en) 2011-05-31
DK2076260T3 (en) 2011-06-27
CN101534820A (en) 2009-09-16
JP5567339B2 (en) 2014-08-06
UA95975C2 (en) 2011-09-26
ATE502634T1 (en) 2011-04-15
WO2008033567A1 (en) 2008-03-20
US20140113935A1 (en) 2014-04-24
IL197566A0 (en) 2009-12-24
CO6180446A2 (en) 2010-07-19
EP2076260A1 (en) 2009-07-08

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